Skerrow D, Skerrow C J
Exp Cell Res. 1983 Jan;143(1):27-35. doi: 10.1016/0014-4827(83)90105-2.
Epidermal tonofilaments are intermediate filaments with an unusually complex polypeptide chain composition which undergoes profound changes during differentiation. Assessment of the possible functional significance of these changes requires their correlation with defined stages of keratinocyte differentiation. Methods have, therefore, been developed for the isolation of the four keratinocyte subpopulations from human epidermis in high yield and purity without detectable damage to tonofilament chains. Trypsinization at 4 degrees C yielded sheets of granular and horny layers and a suspension of basal and spinous cells. Granular cells were removed from the horny layer sheets by mechanical action and basal cells separated from spinous cells by selective attachment to collagen. The living cell fractions were representative, by morphological and ultrastructural criteria, of their counterparts in situ. Analysis of the keratinocyte subpopulations by SDS-PAGE revealed directly their tonofilament chain composition. Basal cells contain two quantitatively major tonofilament chains (Mr 58000 and 50000). A third major chain (Mr 70000) is only synthesised suprabasally when the cells lose their ability to divide. The Mr 50000 chain is removed before the granular cell stage and several minor chains are present in the spinous and granular cells. Two chains appearing for the first time in horny cells probably result from processing during the terminal stages of differentiation. It is suggested that synthesis of the Mr 70000 chain in suprabasal keratinocytes is normally linked with their loss of mitotic ability. This may be significant in the skin disease psoriasis in which synthesis of the Mr 70000 chain is defective and the epidermis hyperproliferates.
表皮张力细丝是一种中间丝,其多肽链组成异常复杂,在分化过程中会发生深刻变化。评估这些变化可能具有的功能意义需要将其与角质形成细胞分化的特定阶段相关联。因此,已经开发出了一些方法,能够从人表皮中高产率、高纯度地分离出四种角质形成细胞亚群,且不会对角质形成细胞张力细丝链造成可检测到的损伤。在4℃下用胰蛋白酶处理可得到颗粒层和角质层薄片以及基底细胞和棘细胞的悬浮液。通过机械作用从角质层薄片中去除颗粒细胞,通过选择性附着于胶原蛋白将基底细胞与棘细胞分离。从形态学和超微结构标准来看,活细胞部分代表了其原位对应细胞。通过SDS - PAGE分析角质形成细胞亚群可直接揭示其张力细丝链组成。基底细胞含有两条数量上占主要的张力细丝链(分子量58000和50000)。第三条主要链(分子量70000)仅在细胞失去分裂能力时在基底上层合成。分子量50000的链在颗粒细胞阶段之前被去除,并且在棘细胞和颗粒细胞中存在几条次要链。在角质细胞中首次出现的两条链可能是分化终末阶段加工过程的结果。有人提出,基底上层角质形成细胞中分子量70000链的合成通常与其有丝分裂能力的丧失有关。这在皮肤病银屑病中可能具有重要意义,在银屑病中分子量70000链的合成存在缺陷,且表皮过度增殖。